Brian P. Chadwick

4.4k total citations
57 papers, 3.1k citations indexed

About

Brian P. Chadwick is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Brian P. Chadwick has authored 57 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 31 papers in Genetics and 22 papers in Plant Science. Recurrent topics in Brian P. Chadwick's work include Genomics and Chromatin Dynamics (28 papers), Chromosomal and Genetic Variations (21 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (18 papers). Brian P. Chadwick is often cited by papers focused on Genomics and Chromatin Dynamics (28 papers), Chromosomal and Genetic Variations (21 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (18 papers). Brian P. Chadwick collaborates with scholars based in United States, United Kingdom and Israel. Brian P. Chadwick's co-authors include Huntington F. Willard, Anna‐Maria Frischauf, Anna-Maria Frischauf, Taiping Chen, Jeremy M. Boss, Parimal Majumder, En Li, Yi Zhang, Jia Fang and Deanna C. Tremblay and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Brian P. Chadwick

57 papers receiving 3.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Brian P. Chadwick United States 28 2.3k 993 605 309 196 57 3.1k
H.F. Willard Canada 26 2.1k 0.9× 895 0.9× 518 0.9× 281 0.9× 112 0.6× 49 3.3k
Heather E. McDermid Canada 29 2.1k 0.9× 2.0k 2.0× 712 1.2× 177 0.6× 59 0.3× 64 3.3k
Maurizio D’Esposito Italy 34 2.9k 1.2× 1.2k 1.2× 180 0.3× 249 0.8× 116 0.6× 67 3.8k
Françis Poulat France 31 2.6k 1.1× 2.4k 2.4× 153 0.3× 198 0.6× 126 0.6× 74 3.6k
Michael J. Friez United States 25 1.7k 0.7× 1.6k 1.6× 161 0.3× 95 0.3× 101 0.5× 82 3.1k
A.S. Henderson United States 28 1.9k 0.8× 802 0.8× 728 1.2× 141 0.5× 422 2.2× 75 3.3k
Michihiko Ito Japan 26 1.3k 0.5× 1.2k 1.2× 244 0.4× 95 0.3× 317 1.6× 81 2.3k
Enrico Moro Italy 33 2.2k 0.9× 1.4k 1.5× 162 0.3× 135 0.4× 65 0.3× 71 3.3k
Elfride De Baere Belgium 39 3.1k 1.3× 1.8k 1.9× 238 0.4× 307 1.0× 56 0.3× 153 4.4k
Giovanna Camerino Italy 34 4.8k 2.1× 5.0k 5.0× 378 0.6× 269 0.9× 182 0.9× 73 6.9k

Countries citing papers authored by Brian P. Chadwick

Since Specialization
Citations

This map shows the geographic impact of Brian P. Chadwick's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Brian P. Chadwick with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brian P. Chadwick more than expected).

Fields of papers citing papers by Brian P. Chadwick

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brian P. Chadwick. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Brian P. Chadwick. The network helps show where Brian P. Chadwick may publish in the future.

Co-authorship network of co-authors of Brian P. Chadwick

This figure shows the co-authorship network connecting the top 25 collaborators of Brian P. Chadwick. A scholar is included among the top collaborators of Brian P. Chadwick based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Brian P. Chadwick. Brian P. Chadwick is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Chadwick, Brian P., et al.. (2021). Deletion of the XIST promoter from the human inactive X chromosome compromises polycomb heterochromatin maintenance. Chromosoma. 130(2-3). 177–197. 3 indexed citations
2.
Huntley, Miriam, Olga Dudchenko, Elena K. Stamenova, et al.. (2016). Deletion of DXZ4 on the human inactive X chromosome alters higher-order genome architecture. Proceedings of the National Academy of Sciences. 113(31). E4504–12. 181 indexed citations
3.
4.
Chadwick, Brian P., et al.. (2014). A novel tRNA variable number tandem repeat at human chromosome 1q23.3 is implicated as a boundary element based on conservation of a CTCF motif in mouse. Nucleic Acids Research. 42(10). 6421–6435. 9 indexed citations
5.
Tremblay, Deanna C., Shawn C. Moseley, & Brian P. Chadwick. (2011). Variation in Array Size, Monomer Composition and Expression of the Macrosatellite DXZ4. PLoS ONE. 6(4). e18969–e18969. 20 indexed citations
6.
Tremblay, Deanna C., et al.. (2010). Expression, tandem repeat copy number variation and stability of four macrosatellite arrays in the human genome. BMC Genomics. 11(1). 632–632. 32 indexed citations
7.
Chadwick, Brian P.. (2009). Macrosatellite epigenetics: the two faces of DXZ4 and D4Z4. Chromosoma. 118(6). 675–681. 21 indexed citations
8.
9.
Chadwick, Brian P. & Huntington F. Willard. (2003). SETting the Stage. Developmental Cell. 4(4). 445–447. 8 indexed citations
10.
Chadwick, Brian P.. (2003). Chromatin of the Barr body: histone and non-histone proteins associated with or excluded from the inactive X chromosome. Human Molecular Genetics. 12(17). 2167–2178. 110 indexed citations
11.
Slaugenhaupt, Susan A., Anat Blumenfeld, Sandra Gill, et al.. (2001). Tissue-Specific Expression of a Splicing Mutation in the Gene Causes Familial Dysautonomia. The American Journal of Human Genetics. 68(3). 598–605. 448 indexed citations
12.
Chadwick, Brian P.. (2001). Histone H2A variants and the inactive X chromosome: identification of a second macroH2A variant. Human Molecular Genetics. 10(10). 1101–1113. 143 indexed citations
13.
Chadwick, Brian P., Maire Leyne, Sandra Gill, et al.. (2000). Cloning, mapping, and expression of a novel brain-specific transcript in the Familial Dysautonomia candidate region on Chromosome 9q31. Mammalian Genome. 11(1). 81–83. 5 indexed citations
14.
Chadwick, Brian P., James Mull, Sandra Gill, et al.. (1999). Cloning, Mapping, and Expression of Two Novel Actin Genes, Actin-like-7A (ACTL7A) and Actin-like-7B (ACTL7B), from the Familial Dysautonomia Candidate Region on 9q31. Genomics. 58(3). 302–309. 32 indexed citations
15.
Chadwick, Brian P., Lynda J. Campbell, Cynthia L. Jackson, et al.. (1999). REPORT on the Sixth International Workshop on Chromosome 9 held at Denver, Colorado, U.S.A., 27 October 1998. Annals of Human Genetics. 63(2). 101–117. 97 indexed citations
16.
Chadwick, Brian P., Thomas Kidd, John Sgouros, David Ish‐Horowicz, & A.-M. Frischauf. (1999). Cloning, mapping and expression of UBL3, a novel ubiquitin-like gene. Gene. 233(1-2). 189–195. 12 indexed citations
17.
18.
Povey, Sue, Brian P. Chadwick, J Frézal, et al.. (1997). REPORT on the Fifth International Workshop on Chromosome 9 held at Eynsham, Oxfordshire, UK, September 4–6, 1996. Annals of Human Genetics. 61(3). 183–206. 25 indexed citations
19.
Chadwick, Brian P., Franz Obermayr, & Anna-Maria Frischauf. (1997). FKHL15,a New Human Member of the Forkhead Gene Family Located on Chromosome 9q22. Genomics. 41(3). 390–396. 53 indexed citations
20.
Chadwick, Brian P., Franz Obermayr, & Anna‐Maria Frischauf. (1996). Nuclear Cap Binding Protein Maps Close to the Xeroderma Pigmentosum Complementation Group A (XPA) Locus in Human and Mouse. Genomics. 35(3). 632–633. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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